Canonical Allele Identifier: CA399657097
Gene: G6PC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008763
ClinVar RCV Id: RCV002816675
dbSNP Id: rs2056094149
gnomAD v4: 17-42911280-G-A
MyVariant Identifiers: chr17:g.41063297G>A (hg19) chr17:g.42911280G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911280G>A , CM000679.2:g.42911280G>A GRCh38
NC_000017.10:g.41063297G>A , CM000679.1:g.41063297G>A GRCh37
NC_000017.9:g.38316823G>A NCBI36
NG_011808.1:g.15483G>A , LRG_147:g.15483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.928G>A MANE Select ENSP00000253801.1:p.Asp310Asn
ENST00000253801.6:c.928G>A ENSP00000253801.1:p.Asp310Asn
ENST00000585489.1:c.*320G>A ENSP00000466202.1:n.*320G>A
ENST00000592383.5:c.*320G>A ENSP00000465958.1:n.*320G>A
NM_000151.3:c.928G>A NP_000142.2:p.Asp310Asn
NM_001270397.1:c.*320G>A NP_001257326.1:n.*320G>A
NM_000151.4:c.928G>A MANE Select NP_000142.2:p.Asp310Asn
NM_001270397.2:c.*320G>A NP_001257326.1:n.*320G>A
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